Method for stabilizing an organic material using a hindered piperidine compound

ABSTRACT

A hindered piperidine compound represented by the formula of ##STR1## wherein R 1  is a 2,2,6,6-tetramethyl-4-piperidyl group of which the N-position is substituted or not, a hydrogen atom, a C 1  -C 18  alkyl group which may contain a cyclic portion, or a C 7  -C 18  arylalkyl group, R 2  is a hydrogen atom, a C 1  -C 10  alkyl group which may contain a cyclic portion, a C 1  -C 18  alkyloxy group which may contain a cyclic portion, or a hydroxyl group, and n is an integer of 2 to 8, effectively stabilizes organic materials having a property to deteriorate by the action of light. A method for producing the compound represented by the above formula is also disclosed.

This is a divisional of application No. 08/056,880 filed May 5, 1993 now U.S. Pat. No. 5,384,348, issued Jan. 24, 1995.

The present invention relates to the stabillzation of organic materials by incorporating a particular hindered piperidine compound into the organic materials, novel hindered piperidine compounds and production of some of the compounds.

It is known that organic materials such as various synthetic resins, including polyethylene, polypropylene, polyvinyl chloride, polyurethane and ABS resins, natural or synthetic rubbers, paints and the like deteriorate by the action of light, and as a result that their physical properties show a large reduction accompanied by phenomena such as softening, embrittlement or discoloration. Because of this, various light stabilizers have so far been developed and used, but demands for novel and more superior light stabilizers are still strong even now. Particularly, developments of light stabilizer compounds having a hindered piperidine skeleton, i.e. a 2,2,6,6-tetramethyl-4-piperidyl group, are actively tried.

For example, EP-A-34829 discloses a compound having a 2,2,6,6-tetramethyl-4-aminopiperidine skeleton and besides forming a carboxylic acid salt, particularly a nickel salt at another site. However, the nickel salt shown here is green, and such coloration of the compound itself is a serious hindrance to use of the compound as a light stabilizer for organic materials.

Further, the above EP-A-34829 discloses a method for producing a lower alkyl ester of the piperidine compound before forming the salt by subjecting 4-alkylamino-2,2,6,6-tetramethylpiperidine or N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)alkylenediamine to Michael reaction with an acrylic acid ester. This method, however, has a drawback that the yield of the desired compound lowers when the acrylic acid ester used has a sterically bulky substituent.

The present inventors have continued a study to develop a stabilizer exhibiting excellent stabilizing effect against the deterioration of organic materials by photo-oxidation, and as a result have found that a particular hindered piperidine compound has excellent effect. The present inventors thus attained to the present invention.

An object of the present invention is to provide a compound having such properties that it exhibits a high stabilizing effect against the deterioration of organic materials by photo-oxidation, and also it itself is white to colorless, giving no color to the organic materials to be stabilized when added thereto.

Another object of the present invention is to stabilize organic materials with such compound.

A further object of the present invention is to produce useful compounds among such compounds in good yields.

According to the present invention, there is provided a particular hindered piperidine compound used as a stabilizer for organic materials. This hindered piperidine compound is represented by the following formula (I): ##STR2## wherein R¹ is a 2,2,6,6-tetramethyl-4-piperidyl group of which the N-position is substituted or not, a hydrogen atom, a C₁ -C₁₈ alkyl group which may contain a cyclic portion, or a C₇ -C₁₈ arylalkyl group; R² is a hydrogen atom, a C₁ -C₁₀ alkyl group which may contain a cyclic portion, a C₁ -C₁₈ alkyloxy group which may contain a cyclic portion, or a hydroxyl group; and n is an integer of 2 to 8.

Thus, the present invention provides a method for stabilizing organic materials by blending them with a stabilizing amount of the hindered piperidine compound represented by the above formula (I), and also provides stabilized organic material compositions comprising the organic materials and the hindered piperidine compound represented by the above formula (I).

The compound of the formula (I) wherein R¹ is a 2,2,6,6-tetramethyl-4-piperidyl group of which the N-position is substituted or not, a C₅ -C₁₈ alkyl group which may contain a cyclic portion or a C₇ -C₁₈ arylalkyl group is a novel compound. Thus, the present invention further provides a hindered piperidine compound represented by the formula (I), wherein R¹ is a 2,2,6,6-tetramethyl-4-piperidyl group of which the N-position is substituted or not, a C₅ -C₁₈ alkyl group which may contain a cyclic portion, or a C₇ -C₁₈ arylalkyl group, and R² and n are as defined above.

Further, according to the present invention, there is provided a method for producing the hindered piperidine compound represented by the formula (I) by transesterification, in which formula R¹ is a 2,2,6,6-tetramethyl-4-piperidyl group of which the N-position is substituted or not, a C₃ -C₁₈ alkyl group which may contain a cyclic portion, or a C₇ -C₁₈ arylalkyl group, and R² and n are as defined above.

In the aforementioned formula (I) representing the hindered piperidine compound which is the stabilizer component of the present invention, R¹ is a 2,2,6,6-tetramethyl-4-piperidyl group of which the N-position is substituted or not, a hydrogen atom, a C₁ -C₁₈ alkyl group which may contain a cyclic portion, or a C₇ -C₁₈ arylalkyl group. When R¹ is a 2,2,6,6-tetramethyl-4-piperidyl group, a substituent bonded to the N-position includes C₁ -C₁₀ alkyl groups which may contain a cyclic portion, C₁ -C₁₈ alkyloxy groups which may contain a cyclic portion, and a hydroxyl group. The 2,2,6,6-tetramethyl-4-piperidyl group, therefore, is generally represented by the following formula (II), ##STR3## wherein R³ is a hydrogen atom, a C₁ -C₁₀ alkyl group which may contain a cyclic portion, a C₁ -C₁₈ alkyloxy group which may contain a cyclic portion, or a hydroxyl group.

When R³ in the formula (II) is an alkyl group having 3 or more carbon atoms, the alkyl group may be of either a straight-chain form or a branched form and also may contain a cyclic portion. A preferred alkyl group containing a cyclic portion and represented by R³ includes those containing a cyclic alkyl group at the middle or terminal and bonding to the nitrogen atom through --CH₂ --. Particularly preferred examples are a cyclohexylmethyl group and a cyclohexylethyl group. Similarly, when R³ in the formula (II) is an alkyloxy group having 3 or more carbon atoms, the alkyl moiety of the group may be of either a straight-chain form or branched form and also may contain a cyclic portion. The alkyloxy group containing a cyclic portion and represented by R³ may be a cyclic alkyloxy group such as cyclohexyloxy. Those which are particularly preferred as R³ in the formula (II) include hydrogen, a C₁ -C₃ alkyl, octyloxy, cyclohexyloxy and the like.

When R¹ in the formula (I) is an alkyl group, it includes, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, n-hexyl, cyclohexyl, n-octyl, 2-ethylhexyl, n-decyl, n-dodecyl, n-octadecyl and the like. Among these alkyl groups, those having 3 or more carbon atoms may be of either a straight-chain form, branched form or cyclic form. When R¹ is an arylalkyl group, it includes, for example, benzyl, phenethyl and the like.

Among these R¹ s, preferred ones include 2,2,6,6-tetramethyl-4-piperidyl, 1,2,2,6,6-pentamethyl-4-piperidyl, 2,2,6,6-tetramethyl-1-octyloxy-4-piperidyl, 1-cyclohexyloxy-2,2,6,6-tetramethyl-4-piperidyl, 1-hydroxy-2,2,6,6-tetramethyl-4-piperidyl, hydrogen, methyl, ethyl, 2-ethylhexyl and the like.

The group R² in the formula (I) is a hydrogen atom, a C₁ -C₁₀ alkyl group which may contain a cyclic portion, a C₁ -C₁₈ alkyloxy group which may contain a cyclic portion, or a hydroxyl group. When R² is an alkyl group, it may be methyl, ethyl, propyl or the like. When the alkyl group has 3 or more carbon atoms, it may be of either a straight-chain form or branched form and also may contain a cyclic portion. A preferred alkyl group containing a cyclic portion and represented by R² includes those containing a cyclic alkyl group at the middle or terminal and bonding to the nitrogen atom through --CH₂ --. Particularly preferred examples are a cyclohexylmethyl group and a cyclohexylethyl group. When R² is an alkyloxy group, it may be, for example, methoxy, ethoxy, hexyloxy, octyloxy or the like. Similarly, when the alkyloxy group has 3 or more carbon atoms, its alkyl moiety may be of either a straight-chain form or branched form and also may contain a cyclic portion. The alkyloxy group containing a cyclic portion and represented by R² may be a cyclic alkyloxy group such as cyclohexyloxy. Among these R² s, preferred ones include hydrogen, a C₁ -C₃ alkyl, octyloxy, cyclohexyloxy and hydroxyl.

The symbol n in the formula (I) is an integer of 2 to 8, and alkylene represented by --C_(n) H_(2n) -- may be of either a straight-chain form or branched form. Specific examples of alkylene represented by --C_(n) H_(2n) -- include ethylene, 1,2- or 1,3-propylene, 1,2-, 1,3- or 1,4-butylene, pentamethylene, hexamethylene, octamethylene and the like. Particularly preferably, n is 6, i.e. --C_(n) C_(2n) -- is hexamethylene.

Among the hindered piperidine compounds represented by the formula (I), particularly useful ones as a stabilizer are compounds in which R¹ is 2,2,6,6-tetramethyl-4-piperidyl, 1,2,2,6,6-pentamethyl-4-piperidyl, 2,2,6,6-tetramethyl-1-octyloxy-4-piperidyl, methyl, 2-ethylhexyl or hydrogen, R² is hydrogen, methyl, methoxy or octyloxy and n is 6. Among these, compounds in which R¹ is 4-piperidyl or methyl and R² is hydrogen are particularly preferred.

In the aforementioned EP-A-34829, particularly in Example 3 thereof, there is disclosed a method for producing one of the compounds represented by the foregoing formula (I), i.e. a compound wherein R¹ is methyl and R² is hydrogen, by subjecting N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine and methyl acrylate together to Michael reaction. According to the method described above, hindered piperidine compounds represented by the formula (I), particularly those in which R¹ is a lower alkyl group, can be produced. That is, a hindered piperidine compound represented by the formula (I) is obtained by Michael reaction of an alkylenediamine compound represented by the formula (III), ##STR4## wherein R² and n are as defined above, and an acrylic acid ester represented by the formula (IV), ##STR5## wherein R¹ is as defined above.

Specific examples of the alkylenediamine compound represented by the formula (III) include the following:

N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-ethylenediamine,

N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,4-butanediamine,

N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,8-octanediamine,

N,N'-bis(1,2,2,6,6-pentamethyl-4-piperidyl)-1,6-hexanediamine,

N,N'-bis(1-hydroxy-2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

N,N'-bis(1-methoxy-2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

N,N'-bis(2,2,6,6-tetramethyl-1-octyloxy-4-piperidyl)-1,6-hexanediamine and the like.

Specific examples of the acrylic acid ester represented by the formula (IV) include methyl acrylate, ethyl acrylate and the like. Among these, methyl acrylate is particularly preferably used.

Usually, it is preferred to carry out the reaction of the alkylenediamine compound of the formula (III) with the acrylic acid ester of the formula (IV) in a solvent. The preferred solvent includes alcohols such as methanol, ethanol, isopropanol and butanol, aromatic hydrocarbons such as benzene, toluene and mesitylene, chlorinated hydrocarbons such as chloroform and carbon tetrachloride, ethers such as tetrahydrofuran and 1,4-dioxane, and the like. Among these, methanol is preferably used particularly when the compound of the formula (IV) is methyl acrylate.

In this reaction, it is preferred to use the acrylic acid ester (IV) in an amount of from about twice by mole to a slight excess based on the alkylenediamine compound (III). More generally, the amount of the acrylic acid ester (IV) per mole of the alkylenediamine compound (III) is preferably in the range of from about 2 to about 4 moles, more preferably in the range of from about 2.0 to about 2.5 moles. Usually, this reaction proceeds in the range of from about 20° C. to refluxing temperature, but preferably it is carried out under reflux. This reaction usually proceeds under an atmospheric pressure, but it may be carried out under pressure.

In the method with Michael reaction, the acrylic acid ester (IV) reacts with the alkylenediamine compound (III) in relatively good efficiency to give the hindered piperidine compound (I) if R¹ in the formula (IV) representing the acrylic acid ester is a lower alkyl group of about the same bulkiness as that of methyl, ethyl, propyl and, at most, butyl. It was found, however, that the yield of the hindered piperidine compound (I) lowers as R¹ in the formula (IV) becomes large in its steric bulkiness. The present inventors, therefore, have extensively studied how to produce the hindered piperidine compound of the formula (I) wherein R¹ is limited, among those defined hereinbefore, to an N-substituted or N-unsubstituted 2,2,6,6-tetramethyl-4-piperidyl group, an alkyl group having 3 or more carbon atoms or an arylalkyl group. As a result, the present inventors have found a method giving an increased yield.

That is, the desired hindered piperidine compound represented by the formula (I) wherein R¹ is an N-substituted or N-unsubstituted 2,2,6,6-tetramethyl-4-piperidyl group, a C₃ -C₁₈ alkyl group which may contain a cyclic portion, or a C₇ -C₁₈ arylalkyl group, can be produced by firstly synthesizing a compound of the formula (I) wherein R¹ is methyl or ethyl, i.e. a lower alkyl ester represented by the formula (Ia), ##STR6## wherein R¹¹ is methyl or ethyl, and R² and n are as defined above, by Michael reaction, if necessary, isolating and purifying the resulting compound (Ia) by the known methods, and then subjecting the isolated and purified product or the reaction mixture and an alcohol represented by the formula (V),

    R.sup.1 OH                                                 (V)

wherein R¹ is an N-substituted or N-unsubstituted 2,2,6,6-tetramethyl-4-piperidyl group, a C₃ -C₁₈ alkyl group which may contain a cyclic portion, or a C₇ -C₁₈ arylalkyl group, to transesterification.

This transesterification is carried out in the presence of a transesterification catalyst. Among the compounds of the formula (I) wherein R¹ is propyl or butyl are also those which can be produced in moderate yields by Michael reaction, but transesterification is more advantageous.

In the lower alkyl ester of the formula (Ia) which is a material for transesterification, a particularly preferred R¹¹ is methyl. Consequently, specific examples of the hindered piperidine compound of the formula (Ia) used in the transesterification include the following:

N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(1,2,2,6,6-pentamethyl-4-piperidyl)-1,6-hexanediamine,

N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-1-octyloxy-4-piperidyl)-1,6-hexanediamine and the like.

Specific examples of the alcohol represented by the formula (V) include 2,2,6,6-tetramethyl-4-piperidinol, 1,2,2,6,6-pentamethyl-4-piperidinol, 2,2,6,6-tetramethyl-1-octyloxy-4-piperidinol, 1-methoxy-2,2,6,6-tetramethyl-4-piperidinol, hexanol, octanol, 2-ethyl-1-hexanol, octadecanol, benzyl alcohol and the like.

Specific examples of the transesterification catalyst include lithium amide, sodium methoxide, potassium methoxide, lithium methoxide, tin oxide and the like.

Usually, it is preferred to carry out the transesterification of the lower alkyl ester of the formula (Ia) with the alcohol of the formula (V) in a solvent. The preferred solvent includes aromatic hydrocarbons such as benzene, toluene, xylene, cymene, monochlorobenzene and o-dichlorobenzene, ethers such as tetrahydrofuran and 1,4-dioxane, and the like.

In this reaction, it is preferred to use the alcohol (V) in an amount of from about twice by mole to a slight excess based on the lower alkyl ester (Ia). More generally speaking, the amount of the alcohol (V) per mole of the lower alkyl ester (Ia) is preferably in the range of from about 2 to about 4 moles, more preferably in the range of from about 2.0 to about 2.5 moles.

In this reaction, it is also preferred to use the transesterification catalyst in an amount ranging from about 0.02 to about 0.2 mole based on mole of the lower alkyl ester (Ia).

This transesterification usually proceeds in the range of from about 20° C. to refluxing temperature, but preferably it is carried out under reflux. Also, this reaction usually proceeds under an atmospheric pressure, but it may be carried out under reduced pressure or under pressure. Further, it is preferred to carry out this reaction While removing a low-boiling alcohol produced with the progress of the reaction out of the reaction system.

The compound of the formula (I) wherein R¹ is a hydroxyl group can be produced by hydrolyzing a compound of the formula (I) wherein R¹ is a lower alkyl group, for example, the lower alkyl ester represented by the formula (Ia).

After Michael reaction of the alkylenediamine compound of the formula (III) with the acrylic acid ester of the formula (IV) has come to an end, the desired hindered piperidine compound of the formula (I) can be isolated by removing the solvent used, or removing the solvent and catalyst when transesterification or hydrolysis has been carried out as need arises. If necessary, a purification operation may further be applied by the known methods.

Any hindered piperidine compound in the scope of the formula (I) can be produced by selecting proper materials and applying the above operation.

Further, if necessary, the groups R² in the formula (I) and/or R³ in the formula (II) can be modified by firstly producing the compound of the formula (I) wherein R¹ is alkyl or arylalkyl and R² is hydrogen, or the compound of the formula (I) wherein R¹ is N-unsubstituted 2,2,6,6-tetramethyl-4-piperidyl and R² is hydrogen, or the compound of the formula (I) wherein R¹ is 4-piperidyl represented by the formula (II) and either one of R² or R³ is hydrogen, and then treating the resulting compound according to the known methods, for example, methods disclosed in EP-A-319,480, U.S. Pat. No. 4,665,185 and particularly Examples 14, 23, 38, 48 and 60 to 65 of EP-A-309,402.

For example, by treating the compound of the formula (I) wherein R¹ is alkyl or arylalkyl and R² is hydrogen with a mixture of formaldehyde and formic acid, R² can be methylated. Also, by treating the compound of the formula (I) wherein R¹ is N-unsubstituted 2,2,6,6-tetramethyl-4-piperidyl and R² is hydrogen with a mixture of formaldehyde and formic acid, the N-position of the 2,2,6,6-tetramethyl-4-piperidyl group and R² can be methylated at the same time. Further, by reacting the compound of the formula (I) wherein R² is hydrogen, or the compound of the formula (I) wherein R¹ is 4-piperidyl represented by the formula (II) and R³ is hydrogen with an oxidizing agent, e.g. hydroperoxide, and then reducing the resulting compound, R² and/or R³ can be converted to a hydroxyl group. Still further, by reacting the compound of the formula (I) wherein R² is hydrogen, or the compound of the formula (I) wherein R¹ is 4-piperidyl represented by the formula (II) and R³ is hydrogen with an alkane or cycloalkane in the presence of an oxidizing agent, an alkyloxy or cycloalkyloxy group can be introduced into R² and/or R³.

Specific examples of the hindered piperidine compound of the formula (I) thus obtained include the following.

Compound A: N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound B: N,N'-bis[2-(2,2,6,6-tetramethyl-4-piperidyloxycarbonyl)ethyl]-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound C: N,N'-bis(2-carboxyethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound D: N,N'-bis(2-ethoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound E: N,N'-bis(2-propoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound F: N,N'-bis(2-isopropoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound G: N,N'-bis(2-butoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound H: N,N'-bis(2-isobutoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound I: N,N'-bis(2-pentyloxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound J: N,N'-bis(2-hexyloxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound K: N,N'-bis(2-cyclohexyloxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound L: N,N'-bis(2-octyloxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound M: N,N'-bis[2-(2-ethylhexyloxycarbonyl)ethyl]-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound N: N,N'-bis(2-dodecyloxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound O: N,N'-bis(2-octadecyloxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound P: N,N'-bis(2-benzyloxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound Q: N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(1,2,2,6,6-pentamethyl-4-piperidyl)-1,6-hexanediamine,

Compound R: N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-1-octyloxy-4-piperidyl)-1,6-hexanediamine,

Compound S: N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(1-hydroxy-2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound T: N,N'-bis[2-(1,2,2,6,6-pentamethyl-4-piperidyloxycarbonyl)ethyl]-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine,

Compound U: N,N'-bis[2-(1,2,2,6,6-pentamethyl-4-piperidyloxycarbonyl)ethyl]-N,N'-bis(1,2,2,6,6-pentamethyl-4-piperidyl)-1,6-hexanediamine,

Compound V: N,N'-bis[2-(2,2,6,6-tetramethyl-4-piperidyloxycarbonyl)ethyl]-N,N'-bis(1,2,2,6,6-pentamethyl-4-piperidyl)-1,6-hexanediamine,

Compound W: N,N'-bis[2-(2,2,6,6-tetramethyl-1-octyloxy-4-piperidyloxycarbonyl)ethyl]-N,N'-bis(2,2,6,6-tetramethyl-1-octyloxy-4-piperidyl)-1,6-hexanediamine,

Compound X: N,N'-bis[2-(2,2,6,6-tetramethyl-4-piperidyloxycarbonyl)ethyl]-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)ethylenediamine,

Compound Y: N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)ethylenediamine.

The hindered piperidine compound represented by the formula (I) is itself a white solid or colorless liquid. This compound is effective to stabilize various kinds of organic material, particularly organic materials having a property to deteriorate by the action of light. Also, this compound does not color the organic materials when added thereto.

The organic material which can be stabilized by the present invention may be any of those having a property to deteriorate by the action of light, there being no special limitation to target organic materials. Specific examples of the material include the following synthetic resins, rubbers, paints, oils and the like. These materials can be stabilized alone or in mixture of two or more of them.

Polyethylene such as low-density polyethylene (LD-PE), high-density polyethylene (HD-PE), and linear low-density polyethylene (LLD-PE);

Polypropylene;

Methylpentene polymer;

EEA (ethylene/ethyl acrylate copolymer) resin;

EVA (ethylene/vinyl acetate copolymer) resin;

polystyrenes such as polystyrene, poly(p-methylstyrene), and poly(α-methylstyrene);

AS (acrylonitrile/styrene copolymer) resin;

ABS (acrylonitrile/butadiene/styrene copolymer) resin;

AAS (special acrylic rubber/acrylonitrile/styrene copolymer) resin;

ACS (acrylonitrile/chlorinated polyethylene/styrene copolymer) resin;

Chlorine-containing polymers such as chlorinated polyethylene, polychloroprene, chlorinated rubber, polyvinyl chloride, and polyvinylidene chloride;

Methacrylic resin;

Ethylene/vinyl alcohol copolymer resin;

Fluorocarbon resin;

Polyacetal;

Grafted polyphenylene ether resin and polyphenylene sulfide resin;

Polyurethane;

Polyamide;

Polyethylene terephthalate and polybutylene terephthalate;

Polycarbonate;

Polyacrylate;

Polysulfone, polyetherether ketone and polyether sulfone;

Aromatic polyester resin;

Epoxy resin;

Diallylphthalate prepolymer;

Silicone resin;

Unsaturated polyester resin;

Acryl-modified benzoguanamine resin;

Benzoguanamine/melamine resin;

Urea resin;

Polybutadiene;

1,2-Polybutadiene;

Polyisoprene;

Styrene/butadiene copolymer;

Butadiene/acrylonitrile copolymer;

Ethylene/propylene copolymer;

Silicone rubber;

Epichlorohydrin rubber;

Acrylic rubber;

Natural rubber;

Chlorinated rubber paint;

Polyester resin paint;

Urethane resin paint;

Epoxy resin paint;

Acrylic resin paint;

Vinyl resin paint;

Aminoalkyl resin paint;

Alkyd resin paint;

Nitrocellulose resin paint;

Oil paint;

Wax; and

Lubricant.

The hindered piperidine compound represented by the formula (I) is blended in a stabilizing amount with organic materials. The preferred amount of the compound varies also with the kind of target organic materials, but it is usually preferred to use the compound in the range of from about 0.01 to about 5 parts by weight based on 100 parts by weight of the organic material. More preferably, the hindered piperidine compound represented by the formula (I) is used in the range of from about 0.02 to about 2 parts by weight based on 100 parts by weight of the organic material.

If necessary, other additives may further be incorporated into organic material compositions obtained by blending the hindered piperidine compound of the formula (I) according to the present invention. Other additives include, for example, phenolic antioxidants, sulfur-containing antioxidants, phosphorus-containing antioxidants, ultraviolet absorbers, hindered amine light stabilizers other than the compound of the formula (I), lubricants, plasticizers, flame retardants, nucleating agents, metal deactivators, antistatic agents, pigments, inorganic fillers and the like. These additives and the hindered piperidine compound of the formula (I) may be blended with organic materials at the same time or at separate steps.

In blending the organic materials with the hindered piperidine compound of the formula (I) and, if necessary, optionally used other additives, all the known methods and apparatus for obtaining a homogeneous mixture may be employed. For example, when the organic material is a solid polymer, these compound and/or additives may be blended with the solid polymer directly or in the form of a master batch. When the organic material is a synthetic polymer, these compound and/or additives may be blended with the polymer by not only the method described above, but also a method in which the solution or dispersion of these compound and/or additives is blended with the solution of the polymer in the course of polymerization of the polymer or immediately after finish of the polymerization. When the organic material is a liquid such as oils, these compound and/or additives may directly be added to dissolve them in the liquid, or may be added in the form of a solution or dispersion in a liquid medium.

The present invention will be explained in more detail with reference to the following examples, but it is not to be interpreted as being limited thereto. All percents and parts in the examples are by weight unless otherwise stated.

EXAMPLE 1 Production of N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine (Compound A)

Eighty grams (0.20 mole) of N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine and 200 g of methanol were added to a 1-liter four-necked flask, and the hexanediamine was completely dissolved in the methanol. To the resulting solution was added dropwise a solution of 35 g (0.41 mole) of methyl acrylate in 100 g of methanol at room temperature. Thereafter, reaction was continued for 12 hours under reflux. After the reaction finished, the solvent was removed by evaporation, and the residue obtained was recrystallized from hexane to obtain 98 g (0.17 mole) of the entitled Compound A as a white solid in a yield of 85%.

Mass analysis (FD-MS): m/z 566 (M)⁺

Elementary analysis (C₃₂ H₆₂ N₄ O₄): Found C 68.1%, H 10.9%, N 10.0% Calcd. C 67.8%, H 11.0%, N 9.9%

m.p. 50°-52° C.

¹ H-NMR (270 MHz, CDCl₃): δ 1.04(dd, J=12.5 and 12.2 Hz, 4H); 1.12(s, 12H); 1.19(s, 12H); 1.2-1.4(m, 4H); 1.4-1.5(m, 4H); 1.63(dd, J=12.5 and 2.9 Hz, 4H); 2.44(t, J=7.1 Hz, 4H); 2.44(t, J=7.2 Hz, 4H); 2.78(t, J=7.2 Hz, 4H); 2.97(tt, J=12.2 and 2.9 Hz, 2H); 3.67(s, 6H) ppm.

EXAMPLE 2 Production of N,N'-bis(2-ethoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine (Compound D)

Procedure was carried out according to Example 1 except that methyl acrylate was replaced by the equimolar amount of ethyl acrylate, to obtain Compound D in a yield of 91%.

Mass analysis (FD-MS): m/z 594 (M)⁺

Elementary analysis (C₃₄ H₆₆ N₄ O₄): Found C 68.7%, H 10.9%, N 9.6% Calcd. C 68.6%, H 11.1%, N 9.4%

m.p. 58°-60° C.

¹ H-NMR (270 MHz, CDCl₃): δ 1.04(dd, J=12.5 and 12.2 Hz, 4H); 1.12(s, 12H); 1.19(s, 12H); 1.2-1.4(m, 4H); 1.26(t, J=7.3 Hz, 6H); 1.4-1.5(m, 4H); 1.62(dd, J=12.5 and 2.9 Hz, 4H); 2.42(t, J=7.1 Hz, 4H); 2.43(t, J=7.1 Hz, 4H); 2.78(t, J=7.1 Hz, 4H); 2.98(tt, J=12.2 and 2.9 Hz, 2H); 4.13(q, J=7.3 Hz, 4H) ppm.

EXAMPLE 3 Production of N,N'-bis(2-octadecyloxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine (Compound O)

To a four-necked flask equipped with a stirrer and a reflux condenser were added 20.0 g (35 mmoles) of N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine (Compound A) obtained in Example 1, 21.0 g (77 mmoles) of stearyl alcohol and 200 ml of toluene, and the resulting mixture was stirred under reflux. To the reaction mixture was added dropwise a solution of 0.1 g (4 mmoles) of lithium amide in 3 g of methanol. Thereafter, the solvent was distilled off while adding toluene, to complete the reaction. After the reaction was continued for 4 hours, toluene was added, and the reaction mixture was cooled to room temperature. The organic layer was washed three times with water and concentrated to obtain 23 g (22 mmoles) of Compound O in a yield of 63%. The yield of Compound O based on N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine was calculated as 54%.

Mass analysis (FD-MS): m/z 1043 (M+1)⁺

Elementary analysis (C₆₆ H₁₃₀ N₄ O₄): Found C 75.9%, H 13.0%, N 5.0% Calcd. C 76.0%, H 12.6%, N 5.4%

m.p. 45°-46° C.

¹ H-NMR (270 MHz, CDCl₃): δ 0.88(t, J=6.6 Hz, 6H); 1.0-1.5(m, 68H); 1.04(dd, J=12.3 and 12.2 Hz, 4H); 1.12(s, 12H); 1.19(s, 12H); 1.6-1.7(m, 4H); 1.63(dd, J=12.2 and 2.6 Hz, 4H); 2.42(t, J=7.1 Hz, 8H); 2.78(t, J=7.1 Hz, 4H); 2.97(tt, J=12.3 and 2.6 Hz, 2H); 4.05(t, J=6.7 Hz, 4H) ppm.

EXAMPLE 4 (for comparison) Production of N,N'-bis(2-octadecyloxycarbonylethyl)-N,N',-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine (Compound O) by Michael reaction

To a 1-liter four-necked flask were added 20 g (50 mmoles) of N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine and 200 g of methanol, and the hexanediamine was completely dissolved in the methanol. To the resulting solution was added dropwise a solution of 32.4 g (0.1 mole) of octadecyl acrylate in 100 g of methanol at room temperature, after which reaction was continued for 12 hours under reflux. The solvent was removed by evaporation, and FD-MS measurement was carried out. As a result, it was found that N-(2-octadecyloxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine was produced in a small amount, but Compound O was not confirmed.

EXAMPLES 5 TO 16 Production of other compounds by transesterification

Procedure was carried out according to Example 3 except using varying alcohols as a material, to obtain the compounds shown in Table 1 in the respective yields. The yields described here are based on Compound A.

                  TABLE 1                                                          ______________________________________                                          ##STR7##                                                                      Example                                                                        No.     Compound    R.sup.1        Yield                                       ______________________________________                                         5       B           2,2,6,6-Tetramethyl-4-                                                                        80%                                                             piperidyl                                                  6       E           n-Propyl       75%                                         7       F           Isopropyl      82%                                         8       G           n-Butyl        77%                                         9       H           Isobutyl       79%                                         10      I           n-Pentyl       54%                                         11      J           n-Hexyl        89%                                         12      K           Cyclohexyl     84%                                         13      L           n-Octyl        92%                                         14      M           2-Ethylhexyl   92%                                         15      N           n-Dodecyl      77%                                         16      P           Benzyl         81%                                         ______________________________________                                    

Compound B:

Mass analysis (FD-MS): m/z 816 (M)⁺

Elementary analysis (C₄₈ H₉₂ N₆ O₄): Found C 70.3%, H 11.4%, N 10.0% Calcd. C 70.5%, H 11.3%, N 10.3%

¹ H-NMR (270 MHz, CDCl₃): δ 1.05(dd, J=12.3 and 12.2 Hz, 4H); 1.13(s, 12H); 1.16(s, 12H); 1.19(s, 12H); 1.23(s, 12H); 1.1-1.5(m, 12H); 1.63(dd, J=12.3 and 2.7 Hz, 4H); 1.93(dd, J=12.5 and 4.2 Hz, 4H); 2.40(t, J=7.4 Hz, 4H); 2.43(t, J=7.6 Hz, 4H); 2.78(t, J=7.4 Hz, 4H); 2.98(tt, J=12.2 and 2.7 Hz, 2H); 5.20(tt, J=11.4 and 4.2 Hz, 2H) ppm.

Compound E:

Mass analysis (FD-MS): m/z 622 (M)⁺

Elementary analysis (C₃₆ H₇₀ N₄ O₄): Found C 69.5%, H 11.1%, N 9.0% Calcd. C 69.4%, H 11.3%, N 9.0%

m.p. 43°-44° C.

¹ H-NMR (270 MHz, CDCl₃): δ 0.95(t, J=7.0 Hz, 6H); 1.04(dd, J=12.5 and 12.2 Hz, 4H); 1.12(s, 12H); 1.19(s, 12H); 1.2-1.3(m, 4H); 1.4-1.5(m, 4H); 1.63(dd, J=12.5 and 3.0 Hz, 4H); 1.6-1.7(m, 4H); 2.43(t, J=7.3 Hz, 8H); 2.78(t, J=7.3 Hz, 4H); 2.98(tt, J=12.2 and 3.0 Hz, 2H); 4.03(t, J=7.0 Hz, 4H) ppm.

Compound F:

Mass analysis (FD-MS): m/z 622 (M)⁺

Elementary analysis (C₃₆ H₇₀ N₄ O₄): Found C 69.2%, H 11.1%, N 9.4% Calcd. C 69.4%, h 11.3%, N 9.0%

¹ H-NMR (270 MHz, CDCl₃): δ 1.04(dd, J=12.5 and 12.2 Hz, 4H); 1.12(s, 12H); 1.19(s, 12H); 1.2-1.3(m, 4H); 1.24(d, J=6.3 Hz, 12H); 1.4-1.5(m, 4H); 1.63(dd, J=12.5 and 3.0 Hz, 4H); 2.39(t, J=7.0 Hz, 4H); 2.42(t, J=7.3 Hz, 4H); 2.77(t, J=7.3 Hz, 4H); 2.98(tt, J=12.2 and 3.0 Hz, 2H); 5.00(hept, J=6.3 Hz, 2H) ppm.

Compound G:

Mass analysis (FD-MS): m/z 650 (M)⁺

Elementary analysis (C₃₈ H₇₄ N₄ O₄): Found C 70.2%, H 11.2%, N 8.7% Calcd. C 70.1%, H 11.5%, N 8.6%

m.p. 66°-67° C.

¹ H-NMR (270 MHz, CDCl₃): δ 0.94(t, J=7.3 Hz, 6H); 0.9-1.1(m, 4H); 1.12(s, 12H); 1.19(s, 12H); 1.2-1.3(m, 4H); 1.3-1.5(m, 8H); 1.6-1.7(m, 8H); 2.42(t, J=7.3 Hz, 8H); 2.78(t, J=7.3 Hz, 4H); 2.97(tt, J=12.2 and 3.1 Hz, 2H); 4.07(t, J=6.6 Hz, 4H) ppm.

Compound H:

Mass analysis (FD-MS): m/z 650 (M)⁺

Elementary analysis (C₃₈ H₇₄ N₄ O₄): Found C 70.2%, H 12.0%, N 8.6% Calcd. C 70.1%, H 11.5%, N 8.6%

m.p. 72°-73° C.

¹ H-NMR (270 MHz, CDCl₃): δ 0.94(d, J=6.6 Hz, 12H); 1.04(dd, J=12.5 and 12.2 Hz, 4H); 1.12(s, 12H); 1.19(s, 12H); 1.2-1.3(m, 4H); 1.4-1.5(m, 4H); 1.63(dd, J=12.5 and 3.0 Hz, 4H); 1.8-2.0(m, 2H); 2.44(t, J=7.3 Hz, 8H); 2.79(t, J=7.3 Hz, 4H); 2.98(tt, J=12.2 and 3.0 Hz, 2H); 3.86(d, J=6.6 Hz, 4H) ppm.

Compound I:

Mass analysis (FD-MS): m/z 678 (M)⁺

Elementary analysis (C₄₀ H₇₈ N₄ O₄): Found C 70.7%, H 11.8%, N 8.3% Calcd. C 70.8%, H 11.6%, N 8.3%

m.p. 36°-37° C.

¹ H-NMR (270 MHz, CDCl₃): δ 0.91(t, J=7.1 Hz, 6H); 0.9-1.1(m, 4H); 1.12(s, 12H); 1.19(s, 12H); 1.2-1.5(m, 16H); 1.6-1.7(m, 8H); 2.42(t, J=7.2 Hz, 8H); 2.78(t, J=7.2 Hz, 4H); 2.97(tt, J=12.4 and 3.1 Hz, 2H); 4.06(t, J=6.9Hz, 4H) ppm.

Compound J:

Mass analysis (FD-MS): m/z 706 (M)⁺

Elementary analysis (C₄₂ H₈₂ N₄ O₄): Found C 71.4%, H 12.0%, N 8.1% Calcd. C 71.3%, H 11.7%, N 8.0%

¹ N-NMR (270 MHz, CDCl₃): δ 0.89(t, J=6.8 Hz, 6H); 0.9-1.1(m, 4H); 1.12(s, 12H); 1.19(s, 12H); 1.2-1.5(m, 20H); 1.6-1.7(m, 8H); 2.42(t, J=7.2 Hz, 8H); 2.78(t, J=7.2 Hz, 4H); 2.97(tt, J=12.2 and 3.0 Hz, 2H); 4.06(t, J=6.8 Hz, 4H) ppm.

Compound K:

Mass analysis (FD-MS): m/z 704 (M)⁺

Elementary analysis (C₄₂ H₇₈ N₄ O₄): Found C 71.6%, H 11.4%, N 8.4% Calcd. C 71.8%, H 11.2%, N 8.0%

¹ H-NMR (270 MHz, CDCl₃): δ 1.04(dd, J=12.5 and 12.2 Hz, 4H); 1.12(s, 12H); 1.19(s, 12H); 1.2-2.0(m, 28H); 1.63(dd, J=12.5 and 3.0 Hz, 4H); 2.40(t, J=7.3 Hz, 4H); 2.43(t, J=6.3 Hz, 4H); 2.78(t, J=7.3 Hz, 4H); 2.98(tt, J=12.2 and 3.0 Hz, 2H); 4.7-4.8(m, 2H) ppm.

Compound L:

Mass analysis (FD-MS): m/z 762 (M)⁺

Elementary analysis (C₄₆ H₉₀ N₄ O₄): Found C 72.1%, H 12.4%, N 7.5% Calcd. C 72.4%, H 11.9%, N 7.4%

¹ H-NMR (270 MHz, CDCl₃): δ 0.88(t, J=6.8 Hz, 6H); 1.04(dd, J=12.5 and 12.2 Hz, 4H); 1.12(s, 12H); 1.19(s, 12H); 1.2-1.5(m, 28H); 1.6-1.7(m, 4H); 1.63(dd, J=12.5 and 2.6 Hz, 4H); 2.42(t, J=7.2 Hz, 8H); 2.78(t, J=7.2 Hz, 4H); 2.97(tt, J=12.2 and 2.6 Hz, 2H); 4.06(t, J=6.8 Hz, 4H) ppm.

Compound M:

Mass analysis (FD-MS): m/z 763 (M+1)⁺

Elementary analysis (C₄₆ H₉₀ N₄ O₄): Found C 72.4%, H 11.5%, N 7.8% Calcd. C 72.4%, H 11.9%, N 7.4%

¹ N-NMR (270 MHz, CDCl₃): δ 0.89(t, J=7.4 Hz, 12H); 1.04(dd, J=12.9 and 12.1 Hz, 4H); 1.12(s, 12H); 1.19(s, 12H); 1.2-1.5(m, 24H); 1.5-1.7(m, 2H); 1.63(dd, J=12.9 and 3.0 Hz, 4H); 2.43(t, J=7.3 Hz, 8H); 2.79(t, J=7.3 Hz, 4H); 2,97(tt, J=12.1 and 3.0 Hz, 2H); 3.98 (dd, J=5.8 and 1.2 Hz, 4H) ppm.

Compound N:

Mass analysis (FD-MS): m/z 874 (M)⁺

Elementary analysis (C₅₄ H₁₀₆ N₄ O₄): Found C 74.0%, H 12.7%, N 6.0% Calcd. C 74.1%, H 12.2%, N 6.4%

¹ N-NMR (270 MHz, CDCl₃): δ 0.88(t, J=6.8 Hz, 6H); 1.04(dd, J=12.3 and 12.2 Hz, 4H); 1.12(s, 12H); 1.19 (s, 12H); 1.2-1.5(m, 40H); 1.6-1.7(m, 8H); 1.63(dd, J=12.2 and 2.5 Hz, 4H); 2.42(t, J=7.2 Hz, 8H); 2.78(t, J=7.2 Hz, 4H); 2.97 (tt, J=12.3 and 2.5 Hz, 2H); 4.05(t, J=6.8 Hz, 4H) ppm.

Compound P:

Mass analysis (FD-MS): m/z 718 (M)⁺

Elementary analysis (C₄₄ H₇₀ N₄ O₄): Found C 73.3%, H 10.3%, N 7.7% Calcd. C 73.5%, H 9.8%, N 7.8%

¹ H-NMR (270 MHz, CDCl₃): δ 1.02(dd, J=12.5 and 12.0 Hz, 4H); 1.10(s, 12H); 1.16(s, 12H); 1.3-1.4(m, 4H); 1.4-1.6(m, 4H); 1.60(dd, J=12.5 and 3.0 Hz, 4H); 2.42(t, J=7.3 Hz, 4H); 2.48(t, J=7.3 Hz, 4H); 2.80(t, J=7.3 Hz, 4H); 2.96(tt, J=12.0 and 3.0 Hz, 2H); 5.11(s, 4H); 7.3-7.5(m, 10H) ppm.

EXAMPLE 17 (for comparison) Production of N,N'-bis(2-n-butoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine (Compound G)

Procedure was carried out according to Example 4 except that octadecyl acrylate was replaced by the equimolar amount of n-butyl acrylate, to obtain Compound G in a yield of 53%.

EXAMPLE 18 Production of N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(1,2,2,6,6-pentamethyl-4-piperidyl)-1,6-hexanediamine (Compound Q)

To a four-necked flask equipped with a stirrer and a reflux condenser were added 3.7 g (41 mmoles) of a 37% aqueous formaldehyde solution, 100 ml of toluene and 1.9 g (41 mmoles) of formic acid. To the resulting mixture was added dropwise a solution of 10 g (17 mmoles) of N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine (Compound A) obtained in Example 1 in 50 ml of toluene. Thereafter, the resulting mixture was refluxed for 3 hours. After the reaction finished, a 5% aqueous sodium hydroxide solution was added to separate the reaction mixture into two layers. The organic layer of the two layers was washed three times with water. The solvent was removed by evaporation to obtain 9 g (15 mmoles) of Compound Q as a viscous liquid in a yield of 88%.

Mass analysis (FD-MS): m/z 594 (M)⁺

Elementary analysis (C₃₄ H₆₆ N₄ O₄): Found C 69.7%, H 11.1%, N 10.2% Calcd. C 68.6%, H 11.2%, N 9.4%

¹ N-NMR (270 MHz, CDCl₃): δ 1.00(s, 12H); 1.14(s, 12H); 1.1-1.6(m, 16H); 2.22(s, 6H); 2.42(t, J=7.0 Hz, 4H); 2.43(t, J=7.0 Hz, 4H); 2.78(t, J=7.0 Hz, 4H); 2.8-2.9(m, 2H); 3.66(s, 6H) ppm.

EXAMPLE 19 Production of N,N'-bis(2-carboxyethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine (Compound C)

To a four-necked flask equipped with a stirrer and a reflux condenser were added 26.3 g (46 mmoles) of N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine (Compound A) obtained in Example 1 and 100 g of water. The resulting mixture was stirred at room temperature. After dissolution of Compound A was confirmed, 100 ml of hexane was added to separate the reaction mixture into two layers. The aqueous layer of the two layers was isolated and concentrated to obtain 23 g (43 mmoles) of Compound C in a yield of 92%.

Mass analysis (FD-MS): m/z 538 (M)⁺

m.p.: >250° C.

Elementary analysis (C₃₀ H₅₈ N₄ O₄): Found C 66.4%, H 10.9%, N 10.2% Calcd. C 66.9%, H 10.9%, N 10.4%

¹ H-NMR (270 MHz, D₂ O): δ 1.3-1.5(m, 4H); 1.37(s, 12H); 1.43(s, 12H); 1.5-1.7(m, 8H), 1.9-2.1(m, 4H); 2.44(t, J=7.6 Hz, 4H); 2.72(t, J=7.8 Hz, 4H); 2.97(t, J=7.6 Hz, 4H); 3.3-3.4(m, 2H) ppm.

EXAMPLE 20 Production of N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(1-hydroxy-2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine (Compound S)

To a four-necked flask equipped with a stirrer and a reflux condenser were added 20.0 g (35 mmoles) of N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine (Compound A) obtained in Example 1, 0.2 g (0.75 mmole) of molybdenum hexacarbonyl and 200 ml of dichloroethane. The resulting mixture was stirred at 60° C. To the reaction mixture was then slowly added dropwise 28 g (248 mmoles) of tert-butyl hydroperoxide, after which reaction was continued for 8 hours under reflux. Inorganic matters were removed by filtration, and the filtrate was washed with a 5% aqueous sodium sulfite solution. The solvent was concentrated, and the product obtained was purified by column chromatography on silica gel (eluent, hexane:ethyl acetate=2:1). Further, the purified product obtained here was added to an autoclave together with 100 ml of dry tetrahydrofuran, 5 g of magnesium sulfate and 2 g of 5% palladium on carbon, and the mixture was stirred at room temperature for 16 hours under a hydrogen pressure of 10 atm. After the solid matter was removed by filtration, the solvent was concentrated, and the product was purified by column chromatography on silica gel (eluent, hexane:ethyl acetate=1:1) to obtain 6 g (10 mmoles) of Compound S in a yield of 28%.

Mass analysis (FD-MS): m/z 598 (M)⁺

Elementary analysis (C₃₂ H₆₂ N₄ O₆): Found C 64.5%, H 10.4%, N 9.6% Calcd. C 64.2%, H 10.4%, N 9.4%

EXAMPLE 21 Weather resistance test of polypropylene

Blending:

    ______________________________________                                         Unstabilized polypropylene                                                                            100    parts                                            Calcium stearate       0.05   part                                             Test Compound          0.1    part                                             ______________________________________                                    

The above blend was melt-kneaded at 230° C. on a 30 mmφ single-screw extruder and pelletized. This pellet was formed into a sheet of 1 mm in thickness at 230° C. on an injection molding machine. This sheet was used as a test piece. This test piece was put in a sunshine weather-O-meter having a light source of carbon arc and irradiated with light under conditions of a black panel temperature being 83° C. and no water spraying. The weather resistance was evaluated by a time which had passed until cracks appeared on the irradiated surface of the test piece.

The results are shown in Table 2.

                  TABLE 2                                                          ______________________________________                                                     Test compound                                                                            Weather resistance                                       ______________________________________                                         Present invention                                                                            Compound A  780 hours                                            Comparison    None        120 hours                                            ______________________________________                                    

EXAMPLE 22 Weather resistance test of polypropylene

Blending:

    ______________________________________                                         Unstabilized propylene/ethylene                                                                        100    parts                                           block copolymer*.sup.1                                                         Calcium stearate        0.05   part                                            Phenolic antioxidant*.sup.2                                                                            0.1    part                                            Phosphorus-containing antioxidant*.sup.3                                                               0.05   part                                            Test compound           0.2    part                                            ______________________________________                                          *.sup.1 Ethylene content of 7.3%                                               *.sup.2                                                                        3,9-Bis[2-{3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propionyloxyy-1,1-dim     thylethyl]-2,4,8,10-tetraoxaspiro[5.5]undecane                                  *.sup.3 Bis(2,4-di-tert-butylphenyl) pentaerythritol diphosphite         

The above blend was melt-kneaded at 230° C. on a 30 mmφ single-screw extruder and pelletized. This pellet was formed into a sheet of 1 mm in thickness at 230° C. on an injection molding machine. This sheet was used as a test piece. This test piece was put in a sunshine weather-O-meter having a light source of carbon arc and irradiated with light under conditions of a black panel temperature being 83° C. and a water spray cycle being 12 minutes/60 minutes. The weather resistance was evaluated by a time which had passed until cracks appeared on the irradiated surface of the test piece. The results are shown in Table 3.

                  TABLE 3                                                          ______________________________________                                          ##STR8##                                                                                                   Life until                                        Run  Compound                cracks appear                                     No.  Symbol   R.sup.1        R.sup.2                                                                              (hour)                                      ______________________________________                                         1    A        Methyl         H     660                                         2    B        2,2,6,6-Tetramethyl-4-                                                                        H     960                                                       piperidyl                                                        3    Q        Methyl         Methyl                                                                               660                                         4    C        H              H     600                                         5    D        Ethyl          H     660                                         6    E        n-Propyl       H     660                                         7    F        Isopropyl      H     660                                         8    G        n-Butyl        H     660                                         9    H        Isobutyl       H     660                                         10   I        n-Pentyl       H     660                                         11   J        n-Hexyl        H     660                                         12   K        Cyclohexyl     H     660                                         13   L        n-Octyl        H     660                                         14   M        2-Ethylhexyl   H     660                                         15   N        n-Dodecyl      H     660                                         16   O        n-Octadecyl    H     600                                         17   P        Benzyl         H     600                                         18   None                    120                                               ______________________________________                                    

The hindered piperidine compound of the present invention gives excellent properties as a stabilizer, particularly as a light stabilizer, to various organic materials including thermoplastic resins such as polyolefin. For example, a resin containing this piperidine compound is stable against photo-oxidation in practical use, and also brings about no color change due to the blending of the compound. Thus, molded products of high quality can be obtained from such a resin. 

What is claimed is:
 1. A method for stabilizing an organic material, comprising the step of blending the organic material with about 0.01 to about 5 parts by weight, based on 100 parts by weight of the organic material, of a hindered piperidine compound represented by formula (I), ##STR9## wherein R¹ is a 2,2,6,6-tetramethyl-4-piperidyl group, a hydrogen atom, a C₁ -C₁₈ alkyl group, or a C₇ -C₁₈ arylalkyl group; R² is a hydrogen atom, a C₁ -C₁₀ alkyl group, a C₁ -C₁₈ alkyloxy group, or a hydroxyl group; and n is an integer of 2 to
 8. 2. The method according to claim 1, wherein R¹ is a 2,2,6,6-tetramethyl-4-piperidyl group.
 3. The method according to claim 2, wherein the N-position of the 2,2,6,6-tetramethyl-4-piperidyl group has no substituent or a substituent selected from the group consisting of a C₁ -C₃ alkyl group, an octyloxy group and a cyclohexyloxy group.
 4. The method according to claim 1, wherein R¹ is a methyl group.
 5. The method according to claim 1, wherein R² is selected from the group consisting of hydrogen, a C₁ -C₃ alkyl group, octyloxy group, a cyclohexyloxy group and a hydroxyl group.
 6. The method according to claim 1, wherein n is
 6. 7. The method according to claim 1, wherein R¹ is selected from the group consisting of a methyl group, an N-unsubstituted 2,2,6,6-tetramethyl-4-piperidyl group, a 1,2,2,6,6-pentamethyl-4-piperidyl group, a 2,2,6,6-tetramethyl-1-octyloxy-4-piperidyl group and a 1-cyclohexyloxy-2,2,6,6-tetramethyl-4-piperidyl group, R² is selected from the group consisting of a hydrogen atom, a C₁ -C₃ alkyl group, an octyloxy group, a cyclohexyloxy group and a hydroxyl group, and n is
 6. 8. The method according to claim 1, wherein the organic material is selected from the group consisting of synthetic resins, rubbers, paints and oils.
 9. The method according to claim 1, wherein the hindered piperidine is blended with the organic material in an amount of about 0.02 to about 2 parts by weight based on 100 parts by weight of the organic material.
 10. The method according to claim 2, wherein the N-position of the 2,2,6,6-tetramethyl-4-piperidyl group has a substituent selected from the group consisting of a C₁ -C₁₀ alkyl group, a C₁ -C₁₈ alkoxy group and a hydroxyl group.
 11. The method according to claim 10, wherein the substituent on the N-position of the 2,2,6,6-tetramethyl-4-piperidyl group is a C₁ -C₁₀ alkyl group.
 12. The method according to claim 10, wherein the substituent on the N-position of the 2,2,6,6-tetramethyl-4-piperidyl group is a C₁ -C₁₈ alkoxy group.
 13. The method according to claim 1, wherein R¹ is a C₁ -C₁₈ alkyl group.
 14. The method according to claim 1, wherein R² is a C₁ -C₁₀ alkyl group.
 15. The method according to claim 1, wherein R² is a C₁ -C₁₈ alkyloxy group.
 16. The method according to claim 11, wherein the C₁ -C₁₀ alkyl group substituent on the N-position of the 2,2,6,6-tetramethyl-4-piperidyl group contains a cyclic alkyl group located at a middle or terminal position of the C₁ -C₁₀ alkyl group, the cyclic alkyl group being bonded to the N-position through one or two --CH₂ -- groups.
 17. The method according to claim 11, wherein the C₁ -C₁₀ alkyl group substituent on the N-position of the 2,2,6,6-tetramethyl-4-piperidyl group is a cyclohexylmethyl group or a cyclohexylethyl group.
 18. The method according to claim 12, wherein the C₁ -C₁₈ alkoxy group substituent on the N-position of the 2,2,6,6-tetramethyl-4-piperidyl group is a cyclic alkoxy group.
 19. The method according to claim 12, wherein the C₁ -C₁₈ alkoxy group substituent on the N-position of the 2,2,6,6-tetramethyl-4-piperidyl group is a cyclohexyloxy group.
 20. The method according to claim 13, wherein the C₁ -C₁₈ alkyl group is a cyclic alkyl group.
 21. The method according to claim 20, wherein the cyclic alkyl group is a cyclohexyl group.
 22. The method according to claim 21, wherein the C₁ -C₁₀ alkyl group contains a cyclic alkyl group located at a middle or terminal portion of the C₁ -C₁₀ alkyl group, the cyclic alkyl group being bonded to the hindered piperidine compound through one or two --CH₂ -- groups.
 23. The method according to claim 14, wherein the C₁ -C₁₀ alkyl group is a cyclohexylmethyl group or a cyclohexylethyl group.
 24. The method according to claim 15, wherein the C₁ -C₁₈ alkyloxy group is a cyclic alkoxy group.
 25. The method according to claim 15, wherein the C₁ -C₁₈ alkyloxy group is a cyclohexyloxy group.
 26. The method according to claim 1, wherein the C₇ -C₁₈ arylalkyl group is a benzyl group or a phenethyl group.
 27. The method according to claim 1, wherein the hindered piperidine compound is N,N'-bis(2-methoxycarbonylethyl)-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine.
 28. The method according to claim 1, wherein the hindered piperidine compound is N,N'-bis[2-(2,2,6,6-tetramethyl-4-piperidyloxycarbonyl)ethyl]-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)-1,6-hexanediamine.
 29. The method according to claim 1, wherein the hindered piperidine compound is N N'-bis(2-methoxycarbonylethyl)-N,N'-bis(1,2,2,6,6-pentamethyl-4-piperidyl)-1,6-hexanediamine.
 30. The method according to claim 1, wherein R¹ is selected from the group consisting of 2,2,6,6-tetramethyl-4-piperidyl, 1,2,2,6,6-pentamethyl-4-piperidyl,2,2,6,6-tetramethyl-1-octyloxy-4-piperidyl, 1-cyclohexyloxy-2,2,6,6-tetramethyl-4-piperidyl, 1-hydroxy-2,2,6,6-tetramethyl-4-piperidyl, hydrogen, methyl, ethyl and 2-ethylhexyl.
 31. The method according to claim 1, wherein R¹ is selected from the group consisting of 2,2,6,6-tetramethyl-4-piperidyl, 1,2,2,6,6-pentamethyl-4-piperidy1,2,2,6,6-tetramethyl-1-octyloxy-4-piperidyl, 1-cyclohexyloxy-2,2,6,6-tetramethyl-4-piperidyl, 1-hydroxy-2,2,6,6-tetramethyl-4-piperidyl, hydrogen, methyl, ethyl and 2-ethylhexyl, R² is selected from the group consisting of a hydrogen atom, a C₁ -C₃ alkyl group, an octyloxy group, a cyclohexyloxy group and a hydroxyl group, and n is
 6. 32. The method according to claim 1, wherein R₁ is a methyl group or a 2,2,6,6-tetramethyl-4-piperidyl group.
 33. The method according to claim 1, wherein R₂ is a hydrogen atom or a methyl group.
 34. The method according to claim 6, wherein R₁ is a methyl group or a 2,2,6,6-tetramethyl-4-piperidyl group and R₂ is a hydrogen atom or a methyl group. 